1-Bromohexadecane

Product Information

Molecular Formula:
C16H33Br
Molecular Weight:
305.34
Description
Applications: 1-Bromohexadecane is used in the preparation of soluble carbon nano-onions by covalent functionalization with hexadecyl chains. It is also used to synthesize [2-(methacryloyloxy)ethyl]dimethylhexadecylammonium bromide monomer, required for the synthesis of novel methacrylate based adsorbents.
Synonyms
1-bromohexadecane
IUPAC Name
1-bromohexadecane
Canonical SMILES
CCCCCCCCCCCCCCCCBr
InChI
InChI=1S/C16H33Br/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h2-16H2,1H3
InChI Key
HNTGIJLWHDPAFN-UHFFFAOYSA-N
Boiling Point
336 ℃
Melting Point
17.3 ℃
Purity
95 %
Density
0.999 g/cm3
Appearance
Clear to yellow liquid
Storage
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
Refractive Index
n20/D 1.461 (lit.)
LogP
6.86260

Safety Information

Hazards
H315
Precautionary Statement
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
9.2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
14
Exact Mass
304.17656 g/mol
Monoisotopic Mass
304.17656 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
123
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114164520-A Preparation method of quaternized silicone rubber fiber and fabric 2022-01-26
CN-114163161-A Modifier for concrete and preparation process thereof 2022-01-21
CN-114176073-A Surface-modifiable nanogel pesticide carrier and construction method thereof 2021-12-06
CN-114181406-A Modified low-protein natural latex with antibacterial effect and preparation method thereof 2021-12-03
CN-114108367-A Method for preparing modified cationic starch by dry method 2021-11-30
CN-113956708-A Water-based ink cleaning agent and preparation method thereof 2021-11-26
CN-113969220-A Water-based UV ink cleaning agent and preparation method thereof 2021-11-26
CN-114181677-A Emulsifier, preparation method and application thereof, and water-in-oil emulsified drilling fluid 2021-11-24
CN-113817009-A Nicotinamide mononucleoside derivative and preparation method and application thereof 2021-11-23
CN-114105776-A Method for synthesizing asymmetric biquaternary ammonium salt 2021-11-23

Literatures

PMID Publication Date Title Journal
22369981 2012-05-15 A method for estimating effective coalescence rates during emulsification from oil transfer experiments Journal of colloid and interface science
22382855 2012-05-07 Determination of endocrine-disrupting phenols in water samples by a new manual shaking-enhanced, ultrasound-assisted emulsification microextraction method The Analyst
22390274 2012-03-05 Advanced biorefinery in lower termite-effect of combined pretreatment during the chewing process Biotechnology for biofuels
22195835 2011-11-30 Bioreducible polycationic micelles for in vitro gene delivery Journal of controlled release : official journal of the Controlled Release Society
21566798 2011-02-10 Synthesis of 1-substituted carbazolyl-1,2,3,4-tetrahydro- and carbazolyl-3,4-dihydro-β-carboline analogs as potential antitumor agents Marine drugs
20625802 2011-01-01 Phenoxazine based units--synthesis, photophysics and electrochemistry Journal of fluorescence
21785613 2011-01-01 Haptenation: chemical reactivity and protein binding Journal of allergy
21117635 2010-12-21 Incorporation and exclusion of long chain alkyl halides in fatty acid monolayers at the air-water interface Langmuir : the ACS journal of surfaces and colloids
20714431 2010-07-19 Multiple beneficial health effects of natural alkylglycerols from shark liver oil Marine drugs
19217119 2009-05-01 Synthesis of novel methacrylate based adsorbents and their sorptive properties towards p-nitrophenol from aqueous solutions Journal of colloid and interface science
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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